NDC 72059-001 Sting Relief Medicated Pad

NDC Product Code 72059-001

NDC 72059-001-01

Package Description: 1 SWAB in 1 PACKET

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Sting Relief Medicated Pad with NDC 72059-001 is a product labeled by Nantong Sirius Packing Products Co., Ltd.. The generic name of Sting Relief Medicated Pad is . The product's dosage form is and is administered via form.

Labeler Name: Nantong Sirius Packing Products Co., Ltd.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nantong Sirius Packing Products Co., Ltd.
Labeler Code: 72059
Start Marketing Date: 02-01-2018 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Sting Relief Medicated Pad Product Label Images

Sting Relief Medicated Pad Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Medicinal Ingredient:Benzocaine6%

Purpose

Topical Anesthetic

Use

For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites

Directions

Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age and older. Children under 2 years: consult a physician.

Warnings

FOR EXTERNAL USE ONLY.FLAMMABLE,Keep away from fire or flame.Do not use in the eyes ,if contact occurs ,flush eyes with water.other information sotre at room temperature 15








OC-30








OC(59-86








OF)

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN. if swallowed get medical help or contact a Poison Control Center right away.

Inactive Ingredients

Isopropyl alcohol,purified water

* Please review the disclaimer below.